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New Pyridine ONN-Pincer Gold and Palladium Complexes:Synthesis,Characterization and Catalysis in Hydrogenation,Hydrosilylation and C-C Cross-Coupling Reactions

机译:新型吡啶ONN-金和钯配合物:加氢,氢化硅烷化和C-C交叉偶联反应的合成,表征和催化

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摘要

The ONN-tridentate unsymmetrical pincer 2-[6-(pyrrolidin-1-ylmethyl)pyridin-2-yl]phenol and N-tert-butyl-1-{[6-(2-hydroxyphenyl)pyridin-2-yl]meth-yl}pyrrolidine-2-carboxamide ligands were synthesized by an easy method in high purity and good yields.All the organic compounds were characterized by elemental analysis,mass spectrometry,IR and ~1H and ~(13)CNMR spectroscopy.Palladium(II)and gold(III)complexes have been prepared as air-stable solids,with the ONN-tridentate ligand after deprotonation of the hydroxy group,the coordination of the metal ion is completely stereospecific and gives rise to only one diastereoisomer.These complexes were shown to be very active catalysts in the hydrogenation(80% ee was achieved with the chiral gold complex),hydrosilylation and C-C coupling,Suzuki and Heck,reactions,under mild conditions.
机译:ONN-三齿不对称钳2- [6-(吡咯烷-1-基甲基)吡啶-2-基]苯酚和N-叔丁基-1-{[[6-(2-羟基苯基)吡啶-2-基]甲基通过简单的方法合成了高纯度,高收率的γ-基}吡咯烷-2-羧酰胺配体。所有的有机化合物均通过元素分析,质谱,IR和〜1H和〜(13)CNMR光谱进行了表征。钯(II )和金(III)配合物已制备为空气稳定的固体,羟基去质子后具有ONN-三齿配体,金属离子的配位是完全立体定向的,仅产生一种非对映异构体。是在温和条件下加氢的非常活泼的催化剂(手性金配合物可实现80%ee),氢化硅烷化和CC偶联,铃木和赫克反应。

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